| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31027055-31027204 | Rare:39 | ||||
| chr14:31206816-31207093 | Common:2; Rare:71 | ||||
| chr14:31207139-31207274 | Rare:39 | ||||
| chr14:31207371-31208023 | Common:2; Rare:202 | ||||
| chr14:31208029-31208471 | Common:2; Rare:105 | ||||
| chr14:31420353-31420803 | Common:7; Rare:136 | ||||
| chr14:31456964-31457105 | Rare:25 | ||||
| chr14:31457162-31457256 | Common:1; Rare:31 | ||||
| chr14:31457264-31457615 | Common:3; Rare:116 | ||||
| chr14:31561088-31561725 | Common:4; Rare:170; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32076086-32076316 | Common:2; Rare:60 | ||||
| chr14:32076497-32077150 | Common:3; Rare:172 | ||||
| chr14:32077247-32077367 | Rare:35 | ||||
| chr14:32077452-32077573 | Rare:49 | ||||
| chr14:32077769-32078052 | Rare:76 |